Publications by authors named "Elif Yilmaz Gulec"

16Publications

Foramina parietalia permagna: familial and radiological evaluation of two cases and review of literature.

Childs Nerv Syst 2017 May 14;33(5):853-857. Epub 2016 Dec 14.

Department of Neurosurgery, Istanbul Bilim University, Sisli Florence Nightingale Hospital, Istanbul, Turkey.

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http://dx.doi.org/10.1007/s00381-016-3315-8DOI Listing
May 2017

Prenatal Diagnosis of Persistent Hyperplastic Primary Vitreous: Report of 2 Cases and Review of the Literature.

J Ultrasound Med 2016 Oct 31;35(10):2285-91. Epub 2016 Aug 31.

Department of Obstetrics and Gynecology, Division of Maternal-Fetal Medicine, Istanbul University, Istanbul Faculty of Medicine, Istanbul, Turkey.

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http://dx.doi.org/10.7863/ultra.15.11040DOI Listing
October 2016

How necessary is to analyze PTPN11 gene in fetuses with first trimester cystic hygroma and normal karyotype?

J Matern Fetal Neonatal Med 2017 Apr 8;30(8):938-941. Epub 2016 Jun 8.

b Department of Maternal Fetal Medicine , Kanuni Sultan Suleyman Training and Research Hospital , Istanbul , Turkey.

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http://dx.doi.org/10.1080/14767058.2016.1191463DOI Listing
April 2017

Genes that Affect Brain Structure and Function Identified by Rare Variant Analyses of Mendelian Neurologic Disease.

Neuron 2015 Nov;88(3):499-513

Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX 77030, USA; Human Genome Sequencing Center, Baylor College of Medicine, Houston, TX 77030, USA; Department of Pediatrics, Baylor College of Medicine, Houston, TX 77030, USA; Texas Children's Hospital, Houston, TX 77030, USA. Electronic address:

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https://linkinghub.elsevier.com/retrieve/pii/S08966273150083
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http://dx.doi.org/10.1016/j.neuron.2015.09.048DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4824012PMC
November 2015

Novel mutations in PTPN11 gene in two girls with Noonan syndrome phenotype.

Int J Cardiol 2015 19;186:13-5. Epub 2015 Mar 19.

Department of Pediatric Neurology, Istanbul Kanuni Sultan Suleyman Training and Research Hospital, Istanbul, Turkey.

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http://dx.doi.org/10.1016/j.ijcard.2015.03.260DOI Listing
January 2016

Cernunnos/XLF Deficiency: A Syndromic Primary Immunodeficiency.

Case Rep Pediatr 2014 8;2014:614238. Epub 2014 Jan 8.

Department of Genetics, Kanuni Sultan Suleyman Research and Training Hospital, 34303 Istanbul, Turkey.

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http://dx.doi.org/10.1155/2014/614238DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3910469PMC
February 2014